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Mouse anti cd2

Manufactured by Bio-Rad
Sourced in United States

Mouse anti-CD2 is a laboratory reagent used for the detection and identification of the CD2 cell surface antigen. CD2 is a glycoprotein expressed on the surface of T cells and natural killer cells, and is involved in cell-cell adhesion and signaling. This product can be used in various immunoassays and flow cytometry applications to study the expression and function of CD2 in biological samples.

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3 protocols using mouse anti cd2

1

Immunostaining of Drosophila Imaginal Discs

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Immunostaining of imaginal discs was performed as previously described (Matakatsu and Blair, 2004 (link)), except that fixations were performed in PBS with 2% formaldehyde for 5 min at RT. The following primary antibodies were used: rat anti–Dachs N and C (1:20,000), guinea pig anti-App (1:20,000; Matakatsu and Blair, 2008 (link)), mouse anti–β-galactosidase (1:1,000; Developmental Studies Hybridoma Bank), rabbit anti–β-galactosidase (1:1,000; Cappel), mouse anti-V5 (1:1,000; Invitrogen), and mouse anti-CD2 (1:1,000; Serotec). Images were taken using an LSM 880 confocal microscope (ZEISS; using Zen 2.1 software) or an Apotome (ZEISS) with an ORCA-ER CCD digital camera (Hamamatsu Photonics). Plan Apochromat 40×/1.4 and Plan Apochromat 63×/1.4 oil-immersion objectives (ZEISS) were used for LSM880. The acquired images were processed with ImageJ and Photoshop (Adobe Systems). Apical z-stacks were processed to make maximal projections using ImageJ.
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2

Imaginal Disc Dissection and Immunostaining

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Imaginal discs were dissected and fixed according to standard protocols. Primary antibodies used were guinea-pig anti-Hth [74 (link)], rabbit anti-PH3 (Sigma), rabbit anti β-galactosidase (Cappel), mouse anti β-galactosidase (Sigma), mouse anti-CD2 (Serotec), rabbit anti-GFP (Molecular Probes), mouse anti-Ey (Clements et al., 2008) and rabbit anti-cyclin B [75 (link)]. Mouse anti-Eya, rat anti-ELAV (7E8A10), and mouse anti-cyclin B were from Developmental Studies Hybridoma Bank (Iowa University). Fluorescently labeled secondary antibodies were from Molecular Probes. Anti-mouse-HRP (Sigma) was used for immunoperoxidase staining. Digoxigenin labelled stg RNA probe was produced from cDNA clone LD47579 (BDGP). ImageJ was used to quantify pixel intensities (http://imagej.nih.gov/ij/).
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3

Immunostaining of Drosophila Larval Discs

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For immunostaining, larval discs were dissected in PBS, fixed in 4% paraformaldehyde, blocked in 5% BSA, and incubated in primary antibodies overnight at 4°C, followed by secondary antibody incubation for 2 h at room temperature. The tissues were mounted with Vectashield mounting medium (Vectashield), and fluorescence images were acquired with a FluoView confocal microscope (Olympus). Primary antibodies used were rabbit anti-phospho-histone3 (Santa Cruz Biotechnology, Santa Cruz, CA, United States; 1:200), mouse anti-CD2 (AbD Serotec, 1:200), rabbit anti-CycE (Santa Cruz Biotechnology, 1:200), and goat anti-Diap1 (Santa Cruz Biotechnology, 1:200); and secondary antibodies were anti-mouse IgG Alexa 488, anti-rabbit IgG Alexa 594, and anti-goat IgG Alexa 594 (Life Technologies, 1:200).
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